Neurodevelopmental Disorder Priority Setting



Survey closed


Help Us Set Priorities For Neurodevelopmental Disorder Research

If you have a neurodevelopmental disorder, or if you care for or work with someone who does, we want you to help us set research priorities for neurodevelopmental research. The goal of this survey is to hear your questions about diagnosis, therapies, care, and other interventions for neurodevelopmental disorders.  Research is vital to finding better ways to improve the health and wellbeing of people living with neurodevelopmental disorders, but researchers can only do this with your help. Tell us about the research questions that are most important to you that still need to be answered. This will help ensure that the work of research funders and researchers focusses on your priorities.

Who should take part in this survey?

People with a neurodevelopmental disorder, their families, their carers, and professionals working with persons who have a neurodevelopmental disorder.

Which neurodevelopmental disorders are included?

  • attention deficient hyperactivity disorder
  • autism spectrum disorder (including  autistic disorder, Asperger’s syndrome, childhood disintegrative disorder, pervasive developmental disorder – not otherwise specified)
  • Down syndrome
  • fragile X
  • intellectual disability
  • obsessive compulsive disorder
  • Rett syndrome
  • Tourette syndrome
  • learning disabilities
  • other genetic syndromes related to intellectual disabilities

How do I access the survey?

The survey is now closed.

What is involved if I take part in the survey?

The survey involves providing us with a few questions you have about diagnosis, therapies, care, and other interventions for neurodevelopmental disorders; as well as few questions help us understand who is completing the survey and make sure we hear from as many Ontarians and perspectives as possible.

What will we do with your questions?

All the questions we receive will be gathered, grouped by topic and checked against published research to see if they have already been answered. If we find answers to any questions we will use this website to ensure the answers are made known to those to whom they will be useful. The questions which have not already been answered will be ranked to find out which are the most important. This process will involve those directly affected by neurodevelopmental disorders, family members, carers, and health care professionals. This process generates a top 10 list of research questions that will be published on the James Lind Alliance and Ontario Brain Institute websites and shared publicly. The James Lind Alliance will facilitate this process and ensure transparency, accountability and fairness.

Who is supporting this survey?

Ontario Brain Institute
The Ontario Brain Institute (OBI) is a provincially-funded, not-for-profit research institution seeking to maximize the impact of neuroscience and establish Ontario as a world leader in brain research, commercialization and care. OBI is financially supporting this priority setting partnership, as well as helping to facilitate the process.
Province of Ontario Neurodevelopmental Disorder Network (POND)
POND is a partner research program of OBI, dedicated to addressing the urgent need for new and better targeted therapies in an effort to improve the long-term outcomes for children with a neurodevelopmental disorder. POND clinicians and patient advisory committee volunteers are helping to support this process by serving on the steering group.
The James Lind Alliance
The James Lind Alliance is a UK-based non-profit coordinated by the National Institute of Health Research ( Its aim is to provide an infrastructure and process to help patients and clinicians work together to agree which are the most important treatment questions affecting their particular interest, in order to influence the prioritisation of future research. The study will be conducted using the methodology set out by the James Lind Alliance. One of their independent advisors will ensure the process is fair, transparent, and representative of each group involved.